BrainEffex: an interactive web application for exploring typical fMRI effect size estimates

Presented During:

Friday, June 27, 2025: 11:30 AM - 12:45 PM
Brisbane Convention & Exhibition Centre  
Room: M3 (Mezzanine Level)  

Poster No:

1822 

Submission Type:

Abstract Submission 

Authors:

Hallee Shearer1, Matt Rosenblatt2, Jean Ye3, Rongtao Jiang4, Link Tejavibulya3, Maya Foster3, Qinghao Liang3, Javid Dadashkarimi5, Margaret Westwater3, Iris Cheng3, Alexandra Fischbach1, Ashley Humphries6, Aneesh Kumar1, Max Rolison3, Hannah Peterson2, Brendan Adkinson4, Saloni Mehta3, Chris Camp3, Thomas Nichols7, Joshua Curtiss1, Dustin Scheinost4, Stephanie Noble1

Institutions:

1Northeastern University, Boston, MA, 2Yale University, New Havent, CT, 3Yale University, New Haven, CT, 4Yale School of Medicine, New Haven, CT, 5Massachusetts General Hospital, Boston, MA, 6University of Nebraska-Lincoln, Lincoln, NE, 7University of Oxford, Oxford, Oxfordshire

First Author:

Hallee Shearer  
Northeastern University
Boston, MA

Co-Author(s):

Matt Rosenblatt  
Yale University
New Havent, CT
Jean Ye  
Yale University
New Haven, CT
Rongtao Jiang  
Yale School of Medicine
New Haven, CT
Link Tejavibulya  
Yale University
New Haven, CT
Maya Foster  
Yale University
New Haven, CT
Qinghao Liang  
Yale University
New Haven, CT
Javid Dadashkarimi  
Massachusetts General Hospital
Boston, MA
Margaret Westwater  
Yale University
New Haven, CT
Iris Cheng  
Yale University
New Haven, CT
Alexandra Fischbach, M.S  
Northeastern University
Boston, MA
Ashley Humphries  
University of Nebraska-Lincoln
Lincoln, NE
Aneesh Kumar  
Northeastern University
Boston, MA
Max Rolison  
Yale University
New Haven, CT
Hannah Peterson  
Yale University
New Havent, CT
Brendan Adkinson, B.S., B.A.  
Yale School of Medicine
New Haven, CT
Saloni Mehta  
Yale University
New Haven, CT
Chris Camp  
Yale University
New Haven, CT
Thomas Nichols, PhD  
University of Oxford
Oxford, Oxfordshire
Joshua Curtiss  
Northeastern University
Boston, MA
Dustin Scheinost  
Yale School of Medicine
New Haven, CT
Stephanie Noble  
Northeastern University
Boston, MA

Introduction:

Estimating effect size is a critical step in power analyses, and can help inform experimental design. However, effect size estimation is particularly difficult for fMRI data due to the complexity of the data and the analysis techniques. Further, it is difficult to obtain estimates from the literature, and small sample sizes of pilot studies may not provide precise enough estimates. When similar studies can be found in the literature, effect sizes are often not reported across the whole brain, limiting utility for study design. To facilitate the estimation and exploration of effect sizes for fMRI, we estimated effects for "typical" study designs with large datasets.

Methods:

Using large (n>500) subject-level datasets provided by contributors, we conducted brain-behavior correlations, task vs. rest contrasts, and between-group analyses with both functional connectivity and task-based activation maps. As of December 2024, the following datasets are included: the Adolescent Brain Cognitive Development study (ABCD), the Human Connectome Project (HCP), the Philadelphia Neurodevelopmental Cohort (PNC), the Healthy Brain Network (HBN), and the UK Biobank (UKB) (Alexander et al., 2017; Casey et al., 2018; Miller et al., 2016; Satterthwaite et al., 2014; Van Essen et al., 2013). The analyses leverage fMRI data from rest and commonly used tasks, and behavioral data reflecting various phenotypes. In light of recent research supporting the promise of broader-level methods (Marek et al., 2022; Noble et al., 2022), we included network-level and multivariate versions of all analyses. We repeated analyses with four motion deconfounding strategies: statistical control, full residualization, thresholding, and no correction. Results were transformed to Cohen's d and R2 estimates of effect size and simultaneous confidence intervals were calculated for each estimate.

Results:

The resulting effect maps from 78 studies were transformed into an interactive web application (BrainEffeX; Figure 1) for exploring, summarizing, and downloading these results (neuroprismlab.shinyapps.io/effect_size_shiny). The analysis pipeline and app were both intentionally designed to support the growth of this resource as more data become available. We welcome contributions of large (n > 500) subject-level fMRI datasets that can be incorporated into BrainEffeX. The structure of data contributions is provided in Figure 2.
Supporting Image: Fig1.jpg
Supporting Image: Fig2.jpg
 

Conclusions:

In summary, BrainEffeX is an interactive Shiny app designed to enable researchers to estimate typical effect sizes for fMRI studies and produce user-relevant summaries of effect size data. This tool is the first to our knowledge to enable users to interactively explore a wide range of "standard" effect sizes in functional neuroimaging. Recognizing that the currently available studies may not address the needs of all users, we have intentionally designed BrainEffeX as a growing resource with plans to incorporate new contributed data as they become available. By providing a reference for expected effect sizes in the field and the development of related tools, BrainEffeX will serve as a springboard for improved study planning and reproducible research in the field.

Modeling and Analysis Methods:

Methods Development 2
Other Methods

Neuroinformatics and Data Sharing:

Databasing and Data Sharing 1
Informatics Other

Novel Imaging Acquisition Methods:

Imaging Methods Other

Keywords:

Computational Neuroscience
Data analysis
Design and Analysis
FUNCTIONAL MRI
Informatics
Multivariate
Open Data
Open-Source Code
Statistical Methods
Other - Effect size

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

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Task-activation

Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Patients

Was this research conducted in the United States?

Yes

Are you Internal Review Board (IRB) certified? Please note: Failure to have IRB, if applicable will lead to automatic rejection of abstract.

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Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

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Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

Not applicable

Please indicate which methods were used in your research:

Functional MRI

Provide references using APA citation style.

Alexander, L. (2017) An open resource for transdiagnostic research in pediatric mental health and learning disorders. Scientific Data, 4(1), 170181. https://doi.org/10.1038/sdata.2017.181

Casey, B. (2018). The Adolescent Brain Cognitive Development (ABCD) study: Imaging acquisition across 21 sites. Developmental Cognitive Neuroscience, 32, 43–54. https://doi.org/10.1016/j.dcn.2018.03.001

Marek, S. (2022). Reproducible brain-wide association studies require thousands of individuals. Nature, 603(7902), 654–660. https://doi.org/10.1038/s41586-022-04492-9

Miller, K. L. (2016). Multimodal population brain imaging in the UK Biobank prospective epidemiological study. Nature Neuroscience, 19(11), 1523–1536. https://doi.org/10.1038/nn.4393

Noble, S. (2022). Improving power in functional magnetic resonance imaging by moving beyond cluster-level inference. Proceedings of the National Academy of Sciences, 119(32), e2203020119. https://doi.org/10.1073/pnas.2203020119

Satterthwaite, T. D. (2014). Neuroimaging of the Philadelphia Neurodevelopmental Cohort. NeuroImage, 86, 544–553. https://doi.org/10.1016/j.neuroimage.2013.0

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